Mr. John Robert Lane PT
Physical Therapist
700 24th St Fort Lee VA, 23801About
John Lane is a physical therapist practicing in Fort Lee, VA. John Lane specializes in physical treatment to help a patient reduce pain, restore mobility, rehabilitate an injury, or increase movement and overall function. As a physical therapist, John Lane can treat multiple conditions with exercises, ultrasound, electrical stimulation, joint mobilization, heat, ice, massage, laser or light therapy and more. John Lane will create a treatment plan based on the patients specific injury or condition, and might target a specific body part or body system based on the individual.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Protean agonism at the dopamine D2 receptor: (S)-3-(3-hydroxyphenyl)-N-propylpiperidine is an agonist for activation of Go1 but an antagonist/inverse agonist for Gi1,Gi2, and Gi3.
- Novel pharmacological applications of G-protein-coupled receptor-G protein fusions.
- Antibodies that identify only the active conformation of G(i) family G protein alpha subunits.
- G protein coupling and ligand selectivity of the D2L and D3 dopamine receptors.
- The 2.6 angstrom crystal structure of a human A2A adenosine receptor bound to an antagonist.
- The endocannabinoid 2-arachidonylglycerol is a negative allosteric modulator of the human A3 adenosine receptor.
- Structure-based discovery of novel chemotypes for adenosine A(2A) receptor antagonists.
- Hybrid ortho/allosteric ligands for the adenosine A(1) receptor.
- Characterization of [3H]LUF5834: A novel non-ribose high-affinity agonist radioligand for the adenosine A1 receptor.
- The structure of the adenosine receptors: implications for drug discovery.
- Mechanism of action of a nanomolar potent, allosteric antagonist of the thyroid-stimulating hormone receptor.
- A Monod-Wyman-Changeux mechanism can explain G protein-coupled receptor (GPCR) allosteric modulation.
- A novel nonribose agonist, LUF5834, engages residues that are distinct from those of adenosine-like ligands to activate the adenosine A(2a) receptor.
- Homobivalent ligands of the atypical antipsychotic clozapine: design, synthesis, and pharmacological evaluation.
- Novel 3,6,7-substituted pyrazolopyrimidines as positive allosteric modulators for the hydroxycarboxylic acid receptor 2 (GPR109A).
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